Rh-Catalyzed C–H alkylation enabling modular synthesis of CF3-substituted benzannulated macrocyclic inhibitors of B cell responses-Reference-Cited by-同舟云学术

Rh-Catalyzed C–H alkylation enabling modular synthesis of CF3-substituted benzannulated macrocyclic inhibitors of B cell responses

Author:

Sun Tao¹²³⁴,He Shijun⁵⁶⁷⁸⁴,Xu Zhongliang⁵⁶⁷⁸⁴,Zuo Jianping⁵⁶⁷⁸⁴,Yu Yang¹²³⁴^ORCID,Yang Weibo⁵⁶⁷⁸⁴^ORCID

Affiliation:

1. Center for Supramolecular Chemistry and Catalysis and Department of Chemistry

2. Shanghai University

3. Shanghai 200444

4. China

5. Chinese Academy of Sciences Key Laboratory of Receptor Research

6. Shanghai Institute of Materia Medica (SIMM)

7. Chinese Academy of Sciences

8. Shanghai

Abstract

Inspired by aspirin and chalcone, herein, we describe a modular biomimetic strategy to achieve a new class of CF₃-bearing benzannulated macrolactams.

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

National Key New Drug Creation and Manufacturing Program, Ministry of Science and Technology

Science and Technology Commission of Shanghai Municipality

Science and Technology Innovation Plan Of Shanghai Science and Technology Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

Reference46 articles.

1. D. J. Newman and G. M.Cragg , The Royal Society of Chemistry , ed. J. Levin , Cambridge , 2015 , vol. 40 , pp. 1–36

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献